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Ctry Approval Spec
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- therapy approvals, viral safety dossiers, import license) in alignment with global
- sites and study are aligned to the critical path for site activation.
- May work with the start-up CRA(s) to prepare the regulatory compliance review
- Entes and maintains trial status information relating to SIA activities onto PPD
- Ensures the local country study files and filing processes are prepared, set up
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